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Developmental Medicine and Child Neurology
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February 5, 2009
The ketogenic diet improves recently worsened focal epilepsy
Nathalie Villeneuve, Florence Pinton, Nadia Bahi-Buisson, et al.
European Journal of Human Genetics : EJHG
|
May 28, 2009
Mutation in the SLC9A6 gene is not a frequent cause of sporadic Angelman-like syndrome
Yann Fichou, Nadia Bahi-Buisson, Juliette Nectoux, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 22, 2010
Developmental and benign movement disorders in childhood
Cecilia Bonnet, Agathe Roubertie, Diane Doummar, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 29, 2018
Polysomnographic findings in Rett syndrome
Alessandro Amaddeo, Livio De Sanctis, Jorge Olmo Arroyo, et al.
Pediatric Neurology
|
February 7, 2006
Misleading effects of clonazepam in symptomatic electrical status epilepticus during sleep syndrome
Nadia Bahi-Buisson, Rosanna Savini, Monica Eisermann, et al.
Neurogenetics
|
November 27, 2008
The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoform
Yann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
American Journal of Medical Genetics. Part A
|
April 29, 2010
Linking MECP2 and pain sensitivity: the example of Rett syndrome
Jenny Downs, Sandrine M Géranton, Ami Bebbington, et al.
European Journal of Human Genetics : EJHG
|
April 5, 2012
The phenotype associated with a large deletion on MECP2
Ami Bebbington, Jenny Downs, Alan Percy, et al.
Molecular Genetics and Metabolism
|
June 12, 2019
Clinical, biochemical and genetic characteristics of a cohort of 101 French and Italian patients with HPRT deficiency
Annalisa Madeo, Maja Di Rocco, Anaïs Brassier, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
November 26, 2010
Cell cloning-based transcriptome analysis in cyclin-dependent kinase-like 5 mutation patients with severe epileptic encephalopathy
Juliette Nectoux, Yann Fichou, Nicolas Cagnard, et al.
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of 18
Search research articles
Search
Showing results (11-20 of 174) with videos related to
Sort By:
Page
of 18
Developmental Medicine and Child Neurology
|
February 5, 2009
The ketogenic diet improves recently worsened focal epilepsy
Nathalie Villeneuve, Florence Pinton, Nadia Bahi-Buisson, et al.
European Journal of Human Genetics : EJHG
|
May 28, 2009
Mutation in the SLC9A6 gene is not a frequent cause of sporadic Angelman-like syndrome
Yann Fichou, Nadia Bahi-Buisson, Juliette Nectoux, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 22, 2010
Developmental and benign movement disorders in childhood
Cecilia Bonnet, Agathe Roubertie, Diane Doummar, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 29, 2018
Polysomnographic findings in Rett syndrome
Alessandro Amaddeo, Livio De Sanctis, Jorge Olmo Arroyo, et al.
Pediatric Neurology
|
February 7, 2006
Misleading effects of clonazepam in symptomatic electrical status epilepticus during sleep syndrome
Nadia Bahi-Buisson, Rosanna Savini, Monica Eisermann, et al.
Neurogenetics
|
November 27, 2008
The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoform
Yann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
American Journal of Medical Genetics. Part A
|
April 29, 2010
Linking MECP2 and pain sensitivity: the example of Rett syndrome
Jenny Downs, Sandrine M Géranton, Ami Bebbington, et al.
European Journal of Human Genetics : EJHG
|
April 5, 2012
The phenotype associated with a large deletion on MECP2
Ami Bebbington, Jenny Downs, Alan Percy, et al.
Molecular Genetics and Metabolism
|
June 12, 2019
Clinical, biochemical and genetic characteristics of a cohort of 101 French and Italian patients with HPRT deficiency
Annalisa Madeo, Maja Di Rocco, Anaïs Brassier, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
November 26, 2010
Cell cloning-based transcriptome analysis in cyclin-dependent kinase-like 5 mutation patients with severe epileptic encephalopathy
Juliette Nectoux, Yann Fichou, Nicolas Cagnard, et al.
Page
of 18